טוען...
Creatine Transporter Deficiency: Screening of Males with Neurodevelopmental Disorders and Neurocognitive Characterization of a Case
OBJECTIVE: Creatine Transporter Deficiency (CTD) is an X-linked, neurometabolic disorder associated with intellectual disability that is characterized by brain creatine deficiency and caused by mutations in SLC6A8, the creatine transporter 1 protein gene. CTD is identified by elevated urine creatine...
שמור ב:
| הוצא לאור ב: | J Dev Behav Pediatr |
|---|---|
| Main Authors: | , , , , , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
2016
|
| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4907372/ https://ncbi.nlm.nih.gov/pubmed/27096572 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/DBP.0000000000000299 |
| תגים: |
הוספת תג
אין תגיות, היה/י הראשונ/ה לתייג את הרשומה!
|